Methods of protein delivery into mammalian cells for gene therapy and genetic studies

dc.contributor.authorTodorova, R.
dc.date.accessioned2012-05-04T12:44:28Z
dc.date.available2012-05-04T12:44:28Z
dc.date.issued2008-06
dc.descriptionAddress for correspondence: R. Todorova Institute of Biophysics Bulgarian Academy of Sciences 1113 Sofia Bulgaria 02 979-31-25 e-mail: todorova@obzor.bio21.bas.bgen_US
dc.description.abstractMethods, lying on different principles for introducing proteins into mammalian cells were compared in the present study. Some of them rely on non-covalent complex formation (Chariot), osmotic lysisis of pinocytic vesicles (Influx pinocytic cell-loading reagent), electric power (electroporation), lipid-based delivery system (Bioporter), microinjection, small protein transduction domains (PTDs) from viral proteins, bacterial secretion system type III (T3SS). Thus, the delivery by many of the compared methods can give a sufficient number of uniformly loaded cells for different studies including transcription and translation, cell cycle regulation, control of apoptosis, oncogenesis and gene therapy.en_US
dc.identifier.citationTodorova, R. Methods of protein delivery into mammalian cells for gene therapy and genetic studies - Acta Medica Bulgarica, 35, 2008, № 1, 3-11.en_US
dc.identifier.issn0324-1750
dc.identifier.urihttp://hdl.handle.net/10861/143
dc.language.isoenen_US
dc.publisherЦентрална медицинска библиотека, МУ София / Central Medical Library - MU Sofiaen_US
dc.subjectprotein delivery, mammalian cells, gene therapy, electroporation, bio-porter, microinjection, nanoparticles, cell-penetrating peptides, pinocytic vesiclesen_US
dc.titleMethods of protein delivery into mammalian cells for gene therapy and genetic studiesen_US
dc.typeArticleen_US
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